
Increased Expression of Capn4 is Associated with the Malignancy of Human Glioma
Author(s) -
Cai JiaJun,
Qi ZengXin,
Hua Wei,
Zhu JingJing,
Zhang Xin,
Yao Yu,
Mao Ying
Publication year - 2014
Publication title -
cns neuroscience and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 69
eISSN - 1755-5949
pISSN - 1755-5930
DOI - 10.1111/cns.12248
Subject(s) - malignancy , glioma , expression (computer science) , cancer research , oncology , medicine , computer science , programming language
Summary Aims Recent evidence indicates that the increased expression of calpain small subunit 1 (Capn4) is associated with tumorigenesis. This study was designed to explore the role which Capn4 plays in human glioma. Methods We detected the expression of Capn4 by immunohistochemistry in tissue microarrays and tissue samples. Following the down‐regulation of Capn4 in glioma cell lines by a specific short hairpin RNA, the function of Capn4 in invasion, migration, and proliferation was assessed. We then evaluated the prognostic role of Capn4 using univariate and multivariate analysis in 94 glioblastoma (GBM) patients. Results Glioma tissues exhibited notably higher expression of Capn4 compared with control brain tissues and was positively correlated with histological malignancy. The down‐regulation of Capn4 in glioma cells led to a decrease in invasion and migration in vitro . Through univariate analysis, the prognosis of GBM patients with Capn4 overexpression was significantly poorer with respect to progression‐free survival (PFS) and overall survival (OS). Based on the results of the multivariate analysis, Capn4 high was demonstrated to be a negative independent prognostic indicator for PFS and OS in GBM patients. Conclusion The overexpression of Capn4 is a novel negative prognostic marker, and Capn4 may be used as a new target in therapeutic strategies for human glioma.